Mapping of clubroot (Plasmodiophora brassicae) resistance in canola (Brassica napus) |
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| Authors: | H. Zhang J. Feng S.‐F. Hwang S. E. Strelkov I. Falak X. Huang R. Sun |
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| Affiliation: | 1. Institute of Vegetables and Flowers, Chinese Academy of Agricultural Sciences, Beijing, China;2. Department of Agricultural, Food and Nutritional Science, University of Alberta, Edmonton, AB, Canada;3. Crop Diversification Centre North, Alberta Agriculture and Rural Development, Edmonton, AB, Canada;4. Pioneer Hi‐Bred Production Ltd, Caledon, ON, Canada |
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| Abstract: | Clubroot disease, caused by Plasmodiophora brassicae, has become a major problem in the production of cruciferous crops worldwide. In this study, a population of 121 doubled haploid (DH) lines derived from a crossing between a resistant and a susceptible canola (Brassica napus) genotype was subjected to phenotypic and genotypic studies to determine the inheritance and location of the resistance gene(s). After inoculation with pathotype 3 of P. brassicae, the lines showed a 1:1 segregation ratio for resistance, indicating that resistance in this population is controlled by a single gene. Fifteen PCR‐based markers that were known to be linked to clubroot resistance (CR) genes were screened against genomic DNA from parents and resistant and susceptible bulks. Marker GC1680, linked to the CR gene CRa, exhibited polymorphism between the parents and between the resistant and susceptible bulks. CRa target primers were used to amplify fragments from the two parents and the resultant sequences were compared. A high degree of sequence similarity was found between the parents in the nucleotide binding site domain of CRa. In contrast, sequence polymorphisms were detected in the leucine‐rich repeat (LRR) domain. One pair of primers that amplify a band from the LRR region of the resistant parent but not the susceptible parent was used to screen the DH population. Amplicons were obtained from 60 of the 61 resistant lines and two of the 60 susceptible lines; thus, three recombinants were found. Based on these results, a resistance locus linked to CRa was found. |
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| Keywords: | bulked segregant analysis genetic markers linkage pathotype QTL |
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